11 дней назад
Clinical Research Associate (Client Dedicated)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Research Associate (Client Dedicated) (Clinical Trials): Conducting site selection, initiation, monitoring, and close-out activities for global clinical trials with an accent on GCP compliance, site quality, recruitment, and regulatory documentation. Focus on tracking trial progress, resolving data queries, training study sites, and managing communication with customers and clinical research stakeholders.
Location: Singapore; hybrid work arrangement
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Perform site selection, initiation, monitoring, and close-out visits while maintaining study documentation.
- Support subject recruitment planning and monitor recruitment progress.
- Establish communication with assigned sites and deliver protocol and study-related training.
- Evaluate site practice quality and integrity, escalating issues when appropriate.
- Track regulatory submissions, case report form completion, and data query resolution.
- Collaborate with colleagues, customers, and clinical research stakeholders across global trials.
Requirements
- University degree in a scientific discipline or healthcare.
- At least one year of on-site monitoring experience.
- Good knowledge of GCP and clinical research regulatory requirements.
- Excellent command of English.
- Good computer skills, including Microsoft Office, plus organizational, time management, and problem-solving skills.
- Ability to build effective working relationships and flexibility to travel.
Culture & Benefits
- Work with different customers on global clinical trials.
- Career development opportunities, mentoring, structured quarterly performance reviews, promotion opportunities, and awards.
- Flexible work schedules and arrangements supported by leaders.
- Training programs covering technical skills, therapeutic knowledge, and regulatory updates.
- Access to in-house technology and an attractive remuneration package.
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